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1-Phenyl-1H-benzotriazole

CAS No.
883-39-6
Chemical Name:
1-Phenyl-1H-benzotriazole
Synonyms
1-phenylbenzotriazole;1-Phenyl-1H-benzotriazole;1H-Benzotriazole, 1-phenyl-;1-Phenyl-1H-benzo[d][1,2,3]triazole
CBNumber:
CB12304572
Molecular Formula:
C12H9N3
Molecular Weight:
195.22
MDL Number:
MFCD01924397
MOL File:
883-39-6.mol
MSDS File:
SDS
Last updated:2026-05-27 23:18:17

1-Phenyl-1H-benzotriazole Properties

Melting point 108-109 °C
Boiling point 359.3±25.0 °C(Predicted)
Density 1.21±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka 0.82±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338

1-Phenyl-1H-benzotriazole price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth AAA88339 1-Phenyl-1H-benzo[d][1,2,3]triazole 883-39-6 1g $337.5 2026-06-04 Buy
Biosynth AAA88339 1-Phenyl-1H-benzo[d][1,2,3]triazole 883-39-6 10g $1875 2026-06-04 Buy
Matrix Scientific 304132 1-Phenyl-1H-benzo[d][1,2,3]triazole 883-39-6 100.00mg $36 2026-05-19 Buy
Matrix Scientific 304132 1-Phenyl-1H-benzo[d][1,2,3]triazole 883-39-6 250.00mg $78 2026-05-19 Buy
Matrix Scientific 304132 1-Phenyl-1H-benzo[d][1,2,3]triazole 883-39-6 1.00g $156 2026-05-19 Buy
Product number Packaging Price Buy
AAA88339 1g $337.5 Buy
AAA88339 10g $1875 Buy
304132 100.00mg $36 Buy
304132 250.00mg $78 Buy
304132 1.00g $156 Buy

1-Phenyl-1H-benzotriazole Chemical Properties, Uses, Production

Uses

1-Phenyl-1H-benzo[d][1,2,3]triazole is a reagent used in the prepartion of possible surrogates for kobayashi’s aryne precursors.

Synthesis

1H-Benzotriazole

95-14-7

Iodobenzene

591-50-4

1-Phenyl-1H-benzotriazole

883-39-6

GENERAL METHODS: Cu(OAc)2-H2O (0.01 mmol) was dissolved in DMF (2 mL) under nitrogen protection, and iodobenzene (1.2 mmol), benzotriazole (1.0 mmol), and Cs2CO3 (2 mmol) were added sequentially. The reaction system was stirred at 110 °C for 24 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was partitioned between water and ethyl acetate. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford the target product 1-phenyl-1H-benzo[d][1,2,3]triazole.

References

[1] Tetrahedron Letters, 1998, vol. 39, # 31, p. 5617 - 5620
[2] RSC Advances, 2015, vol. 5, # 51, p. 40628 - 40635
[3] Synthetic Communications, 2012, vol. 42, # 15, p. 2217 - 2228
[4] Journal of Organic Chemistry, 2004, vol. 69, # 17, p. 5578 - 5587
[5] Synthesis, 2012, vol. 44, # 7, p. 1063 - 1068

1-Phenyl-1H-benzotriazole Preparation Products And Raw materials

1-Phenyl-1H-benzotriazole Suppliers

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1-Phenyl-1H-benzotriazole 1-phenylbenzotriazole 1-Phenyl-1H-benzo[d][1,2,3]triazole 1H-Benzotriazole, 1-phenyl- 883-39-6